| Aprosencephaly cerebellar dysgenesis | |
| Synonym: | Aprosencephaly and cerebellar dysgenesis |
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| Incidence: | or |
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Aprosencephaly cerebellar dysgenesis is a rare, non-syndromic central nervous system malformation characterized by the absence of the telencephalon and diencephalic structures. These are often combined with severe abnormalities in the mesencephalon and cerebellum.[1] [2]
Features of this condition include:
Malformations extending to the hands and feet have also been described.
This condition is genetic, but its origins are unclear. The symptoms presented suggested OTX2 expression, but testing found no variation of OTX2 in patients. This condition is believed to be autosomal recessive.
The condition was first described in 1996.